treatment of bony defect in a back tooth using self and artificial material
- Conditions
- Health Condition 1: K053- Chronic periodontitis
- Registration Number
- CTRI/2023/08/056883
- Lead Sponsor
- ot applicable
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
•Age of the patient – above 25years
•Systemically healthy patient (except for well controlled Type 2 DM).
•Vertical probing pocket depths = 5mm measured with UNC 15 probe four weeks following initial therapy
•Clinical attachment loss = 4mm measured with UNC 15 probe four weeks following initial therapy
•Gingival margin positioned coronally to the furcation fornix
•Patients with thick gingival biotype
•No history of periodontal therapy in the preceding 6months
•No use of antibiotics in the preceding 6months
•Non-smokers
•With known systemic disease
•Use of tobacco in any form and alcohol
•Immunocompromised individuals
•Pregnant or lactating females, along with those taking oral contraceptives.
•Tooth with hopeless prognosis.
•Patients with inadequate compliance with the oral hygiene maintenance schedule.
•Teeth with Grade-III mobility
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method change in horizontal and vertical dimension of the furcation defects baselineTimepoint: 0-6 months
- Secondary Outcome Measures
Name Time Method change in vertical Probing depths, Clinical attachment levels, modified sulcular bleeding index, and Plaque indexTimepoint: 0-3month-6month